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February 15, 1996BloodOpen Access

Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder

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Authors

FTFlorence TotiInsermNSNathalie SattaUniversity of GenevaEFE FressinaudRoche (Switzerland)

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Cite This Study

Toti et al. (1996) studied this question.

synapsesocial.com/papers/6a1bf675bc71fb1015a91ea0https://doi.org/10.1182/blood.v87.4.1409.bloodjournal8741409
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Annexin V as a probe of aminophospholipid exposure and platelet membrane vesiculation: a flow cytometry study showing a role for free sulfhydryl groups1993 · 357 citations
  2. 2Defective Ca(2+)-induced microvesiculation and deficient expression of procoagulant activity in erythrocytes from a patient with a bleeding disorder: a study of the red blood cells of Scott syndrome1992 · 146 citations
  3. 3Vesicular stomatitis virus binds and fuses with phospholipid domain in target cell membranes1986 · 55 citations
  4. 4Differentiation-dependent expression of phosphatidylserine in mammalian plasma membranes: quantitative assessment of outer-leaflet lipid by prothrombinase complex formation.1989 · 186 citations
  5. 5Effect of antiphospholipid antibodies on procoagulant activity of activated platelets and platelet‐derived microvesicles1993 · 89 citations